Canonical Allele Identifier: CA1459091685

Gene: TMEM165

Linked Data

• dbSNP Id: rs534654
• gnomAD v4: 4-55424053-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55424053A>T , CM000666.2:g.55424053A>T	GRCh38
NC_000004.11:g.56290220A>T , CM000666.1:g.56290220A>T	GRCh37
NC_000004.10:g.55984977A>T	NCBI36
NG_032881.1:g.33141A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381334.10:c.793-485A>T MANE Select	ENSP00000370736.5:n.793-485A>T
ENST00000381334.9:c.793-485A>T	ENSP00000370736.5:n.793-485A>T
ENST00000506103.2:c.247-485A>T
ENST00000506198.5:c.208-485A>T	ENSP00000425449.1:n.208-485A>T
ENST00000508404.5:c.*665-485A>T	ENSP00000422639.1:n.*665-485A>T
ENST00000508561.5:n.489-485A>T
ENST00000509575.1:n.296-485A>T
ENST00000514904.5:n.1247-485A>T
ENST00000515591.1:n.940A>T
ENST00000608091.1:c.303-485A>T
NM_018475.4:c.793-485A>T	NP_060945.2:n.793-485A>T
NR_073070.1:n.1173-485A>T
XM_011534394.1:c.793-485A>T	XP_011532696.1:n.793-485A>T
XM_011534394.3:c.793-485A>T	XP_011532696.1:n.793-485A>T
XM_017008412.1:c.604-485A>T	XP_016863901.1:n.604-485A>T
XR_001741287.2:n.1509-485A>T
NM_018475.5:c.793-485A>T MANE Select	NP_060945.2:n.793-485A>T
NR_073070.2:n.1129-485A>T